Canonical Allele Identifier: CA1573491263
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112839521_112839532delinsAAAGATTGGAAC , CM000667.2:g.112839521_112839532delinsAAAGATTGGAAC GRCh38
NC_000005.9:g.112175218_112175229delinsAAAGATTGGAAC , CM000667.1:g.112175218_112175229delinsAAAGATTGGAAC GRCh37
NC_000005.8:g.112203117_112203128delinsAAAGATTGGAAC NCBI36
NG_008481.4:g.152001_152012delinsAAAGATTGGAAC , LRG_130:g.152001_152012delinsAAAGATTGGAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000502371.3:c.3592_3603delinsAAAGATTGGAAC ENSP00000484935.2:n.3592_3603delinsAAAGAT...
ENST00000504915.3:c.3981_3992delinsAAAGATTGGAAC ENSP00000473355.2:p.Glu1327=
ENST00000505350.2:c.*3933_*3944delinsAAAGATTGGAAC ENSP00000481752.1:n.*3933_*3944delinsAAAG...
ENST00000507379.6:c.3873_3884delinsAAAGATTGGAAC ENSP00000423224.2:p.Glu1291=
ENST00000509732.6:c.3927_3938delinsAAAGATTGGAAC ENSP00000426541.2:p.Glu1309=
ENST00000512211.7:c.3927_3938delinsAAAGATTGGAAC ENSP00000423828.3:p.Glu1309=
ENST00000257430.9:c.3927_3938delinsAAAGATTGGAAC MANE Select ENSP00000257430.4:p.Glu1309=
ENST00000257430.8:c.3927_3938delinsAAAGATTGGAAC ENSP00000257430.4:p.Glu1309=
ENST00000502371.2:c.2280_2291delinsAAAGATTGGAAC
ENST00000508376.6:c.3927_3938delinsAAAGATTGGAAC ENSP00000427089.2:p.Glu1309=
ENST00000508624.5:c.*3249_*3260delinsAAAGATTGGAAC ENSP00000424265.1:n.*3249_*3260delinsAAAG...
ENST00000520401.1:c.230+10549_230+10560delinsAAAGATTGGAAC
NM_000038.5:c.3927_3938delinsAAAGATTGGAAC NP_000029.2:p.Glu1309=
NM_001127510.2:c.3927_3938delinsAAAGATTGGAAC NP_001120982.1:p.Glu1309=
NM_001127511.2:c.3873_3884delinsAAAGATTGGAAC NP_001120983.2:p.Glu1291=
NM_001354895.1:c.3927_3938delinsAAAGATTGGAAC NP_001341824.1:p.Glu1309=
NM_001354896.1:c.3981_3992delinsAAAGATTGGAAC NP_001341825.1:p.Glu1327=
NM_001354897.1:c.3957_3968delinsAAAGATTGGAAC NP_001341826.1:p.Glu1319=
NM_001354898.1:c.3852_3863delinsAAAGATTGGAAC NP_001341827.1:p.Glu1284=
NM_001354899.1:c.3843_3854delinsAAAGATTGGAAC NP_001341828.1:p.Glu1281=
NM_001354900.1:c.3804_3815delinsAAAGATTGGAAC NP_001341829.1:p.Glu1268=
NM_001354901.1:c.3750_3761delinsAAAGATTGGAAC NP_001341830.1:p.Glu1250=
NM_001354902.1:c.3654_3665delinsAAAGATTGGAAC NP_001341831.1:p.Glu1218=
NM_001354903.1:c.3624_3635delinsAAAGATTGGAAC NP_001341832.1:p.Glu1208=
NM_001354904.1:c.3549_3560delinsAAAGATTGGAAC NP_001341833.1:p.Glu1183=
NM_001354905.1:c.3447_3458delinsAAAGATTGGAAC NP_001341834.1:p.Glu1149=
NM_001354906.1:c.3078_3089delinsAAAGATTGGAAC NP_001341835.1:p.Glu1026=
NM_000038.6:c.3927_3938delinsAAAGATTGGAAC MANE Select NP_000029.2:p.Glu1309=
NM_001127510.3:c.3927_3938delinsAAAGATTGGAAC NP_001120982.1:p.Glu1309=
NM_001127511.3:c.3873_3884delinsAAAGATTGGAAC NP_001120983.2:p.Glu1291=
NM_001354895.2:c.3927_3938delinsAAAGATTGGAAC NP_001341824.1:p.Glu1309=
NM_001354896.2:c.3981_3992delinsAAAGATTGGAAC NP_001341825.1:p.Glu1327=
NM_001354897.2:c.3957_3968delinsAAAGATTGGAAC NP_001341826.1:p.Glu1319=
NM_001354898.2:c.3852_3863delinsAAAGATTGGAAC NP_001341827.1:p.Glu1284=
NM_001354899.2:c.3843_3854delinsAAAGATTGGAAC NP_001341828.1:p.Glu1281=
NM_001354900.2:c.3804_3815delinsAAAGATTGGAAC NP_001341829.1:p.Glu1268=
NM_001354901.2:c.3750_3761delinsAAAGATTGGAAC NP_001341830.1:p.Glu1250=
NM_001354902.2:c.3654_3665delinsAAAGATTGGAAC NP_001341831.1:p.Glu1218=
NM_001354903.2:c.3624_3635delinsAAAGATTGGAAC NP_001341832.1:p.Glu1208=
NM_001354904.2:c.3549_3560delinsAAAGATTGGAAC NP_001341833.1:p.Glu1183=
NM_001354905.2:c.3447_3458delinsAAAGATTGGAAC NP_001341834.1:p.Glu1149=
NM_001354906.2:c.3078_3089delinsAAAGATTGGAAC NP_001341835.1:p.Glu1026=